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10q11.2
A chromosome band present on 10q
National Institutes of Health
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Related topics
Related topics
9 relations
10q
ALOX5 wt Allele
Chromosomes
DKK1 wt Allele
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2009
Highly Cited
2009
Fine mapping and functional analysis of a common variant in MSMB on chromosome 10q11.2 associated with prostate cancer susceptibility
H. Lou
,
M. Yeager
,
+33 authors
S. Chanock
Proceedings of the National Academy of Sciences
2009
Corpus ID: 12181160
Two recent genome-wide association studies have independently identified a prostate cancer susceptibility locus on chromosome…
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Highly Cited
2003
Highly Cited
2003
Germline PTEN promoter mutations and deletions in Cowden/Bannayan-Riley-Ruvalcaba syndrome result in aberrant PTEN protein and dysregulation of the phosphoinositol-3-kinase/Akt pathway.
Xiao-ping Zhou
,
K. Waite
,
+13 authors
C. Eng
American Journal of Human Genetics
2003
Corpus ID: 18690626
Germline intragenic mutations in PTEN are associated with 80% of patients with Cowden syndrome (CS) and 60% of patients with…
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Highly Cited
1999
Highly Cited
1999
Pharmacogenetic association between ALOX5 promoter genotype and the response to anti-asthma treatment
J. Drazen
,
C. Yandava
,
+8 authors
J. Drajesk
Nature Genetics
1999
Corpus ID: 21991803
Clinically similar asthma patients may develop airway obstruction by different mechanisms. Asthma treatments that specifically…
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Review
1999
Review
1999
RET proto-oncogene in the development of human cancer.
C. Eng
Journal of Clinical Oncology
1999
Corpus ID: 40658036
The RET proto-oncogene, located on chromosome subband 10q11.2, encodes a receptor tyrosine kinase expressed in tissues and tumors…
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Highly Cited
1995
Highly Cited
1995
Diversity of RET proto-oncogene mutations in familial and sporadic Hirschsprung disease.
T. Attié
,
A. Pelet
,
+7 authors
A. Munnich
Human Molecular Genetics
1995
Corpus ID: 12413401
Hirschsprung disease (HSCR) is a common congenital malformation (1 in 5,000 live births) due to the absence of autonomic ganglia…
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Highly Cited
1994
Highly Cited
1994
Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease
G. Romeo
,
P. Ronchetto
,
+8 authors
G. Martucciello
Nature
1994
Corpus ID: 157274
HIRSCHSPRUNG'S disease is a genetic disorder of neural crest development affecting 1 in 5,000 births. It is characterized by the…
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Highly Cited
1994
Highly Cited
1994
Mutations of the RET proto-oncogene in Hirschsprung's disease
P. Edery
,
S. Lyonnet
,
+7 authors
A. Munnich
Nature
1994
Corpus ID: 1361408
HIRSCHSPRUNG'S disease (HSCR)1 is a common condition (1 in 5,000 live births) resulting in intestinal obstruction in neonates2…
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Highly Cited
1994
Highly Cited
1994
Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumours.
C. Eng
,
D. Smith
,
+7 authors
A. Tunnacliffe
Human Molecular Genetics
1994
Corpus ID: 887179
The susceptibility loci for the three multiple endocrine neoplasia (MEN) type 2 syndromes have been mapped to the region of…
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Highly Cited
1992
Highly Cited
1992
Single base polymorphism at −511 in the human interleukin-1β gene (IL1β)
F. Giovine
,
E. Takhsh
,
A. Blakemore
,
G. Duff
1992
Corpus ID: 84978233
F.S. di Giovine*. E.Takhsh, A.I.F.BIakemore and G.W.Duff Section of Molecular Medicine, Department of Medicine and Pharmacology…
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Highly Cited
1989
Highly Cited
1989
Human ret proto-oncogene mapped to chromosome 10q11.2.
Y. Ishizaka
,
F. Itoh
,
+6 authors
M. Nagao
Oncogene
1989
Corpus ID: 9614281
Using cosmid clones derived from human ret protooncogene as probes, we determined its chromosome localization by fluorescence in…
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